Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000204966 Individual ID 00267036 Associated disease ASNSD Phenotype details Microcephaly HP:0000252 Cerebellar hypoplasia HP:0001321 Diagnosis/Initial - Inheritance Familial, autosomal recessive Diagnosis/Definite - Age/Examination - Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Sandra Cooper Database submission license No license selected Created by Sandra Cooper Date created 2019-10-31 03:21:28 +01:00 (CET) Date last edited 2019-10-31 13:57:48 +01:00 (CET)

Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.